A carregar...

Cell-Intrinsic Functional Effects of the α-Cardiac Myosin Arg-403-Gln Mutation in Familial Hypertrophic Cardiomyopathy

Human familial hypertrophic cardiomyopathy is the most common Mendelian cardiovascular disease worldwide. Among the most severe presentations of the disease are those in families heterozygous for the mutation R403Q in β-cardiac myosin. Mice heterozygous for this mutation in the α-cardiac myosin isof...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Chuan, Peiying, Sivaramakrishnan, Sivaraj, Ashley, Euan A., Spudich, James A.
Formato: Artigo
Idioma:Inglês
Publicado em: The Biophysical Society 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3379014/
https://ncbi.nlm.nih.gov/pubmed/22735528
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bpj.2012.04.049
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!